Shape is important in determining the interaction between a drug and a target
true
antagonists have both affinity and efficacy
false
which of these does not represent a drug target, enzyme receptor, lipid, DNA
lipid
albumin, acid glycoprotein and beta-globulin are examples of drug targets
false
partial agonist can elicit a maximum tissue response
false
irreversible antagonists use which type of chemical bond
covalent
drugs with LIMITED plasma protein binding and HIGH lipid solubility will have a large volume of distribution
TRUE
drug metabolism occurs principally in the, liver, lung, stomach, kidney
liver
first pass metabolism affects drugs given IV
false
oxidation, reduction and conjugation are all phase 1 metabolism reactions
false (not conjugation that is a phase 2)
phase 1 metabolites are always more polar and less active than the parent drug
false
a decrease in first pass metabolites results in an increase in bioavailability true
true
rifampicin can speed up the metabolism of the oral contraceptive pill
true (bnf qestion)
grapefruit juice is a key inducer of CYP450 enzymes
false (inhibitor)
drugs bound to plasma proteins are filtered through the glomerular capillaries
false - think too big
drugs which are excreted unchanged via the urine typically have which chemical nature
polar
why are polar drugs excreted easily via the kidney
hydrophillic
a drug with high volume of distribution could be removed from the body rapidly via dialysis
false - too late, not in circulation
a weakly basic drug will be easily excreted in acid urine
true
the half life of a polar drug is increased in renal failure
true
acetylcholine binds to nicotonic, muscarinic and adrenergic receptors
false, not adrenergic
which of the following symptoms could be described as an anti muscarinic side effect? diarrhoea, excessive urination, constipation, bradycardia
constipation
anticholinesterase drugs such as rivastigmine increase cholinergic signalling
true
adrenaline is the primary neurotransmitter in the SNS
false - adrenaline is a hormone